Results 241 to 250 of about 1,574,797 (410)

Spinal Fusion and Instrumentation for Paediatric Neuromuscular Scoliosis: Retrospective Review [PDF]

open access: gold, 2002
Mihir M. Thacker   +4 more
openalex   +1 more source

Spinal fusion surgery: A historical perspective.

open access: yesJournal of Orthopaedics, 2017
S. Tarpada   +2 more
semanticscholar   +1 more source

Exonic Variation and Its Clinical Impact in 7221 Old Order Amish

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The Amish of Lancaster County, PA has been the focus of genetic studies for many years due to its demographic history and unique genetic makeup that includes a historical bottleneck event and subsequent genetic drift, resulting in a marked decrease in genetic diversity and increased frequency of some variants that have substantially shaped the
Braxton D. Mitchell   +21 more
wiley   +1 more source

A Randomized, Controlled Trial of Fusion Surgery for Lumbar Spinal Stenosis.

open access: yesNew England Journal of Medicine, 2016
P. Försth   +8 more
semanticscholar   +1 more source

Sacroiliac Joint Involvement: An Underreported Complication of NF1

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT NF1‐related bone dysplasia in children and young adults with neurofibromatosis type 1 (NF1) involving the sacroiliac joint has been rarely described. We report four participants who underwent whole‐body magnetic resonance imaging (WB‐MRI) as part of a longitudinal imaging and plexiform neurofibroma (PN) biomarker study (NCT05238909) at Ann ...
Jenny P. Garzon   +6 more
wiley   +1 more source

Impact of Habitual Flexion on Bone Formation After Spinal Fusion Surgery: An In Silico Study. [PDF]

open access: yesJOR Spine
Ananth Swaminathan S   +5 more
europepmc   +1 more source

A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss‐of‐Function of DMRT2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Spondylocostal dysostosis (SCDO) is a rare genetic disorder characterized by abnormal development of the axial skeleton, resulting in malformations of the vertebrae and ribs that often impair lung development and lead to significant respiratory morbidity.
Jonathan Rips   +8 more
wiley   +1 more source

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